Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty. La fibrosis quística es un trastorno genético que afecta sobre todo a los pulmones y el sistema digestivo y hace que los niños que la padecen sean más . La mejora durante las últimas décadas de las técnicas de tratamiento y de soporte nutricional de los pacientes con fibrosis quística ha permitido prolongar la.
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Archivos de Bronconeumologia http: Other types of articles such as reviews, editorials, special articles, qutsica reports, and letters to the Editor are also published in the Journal. It is a monthly Journal that publishes a total of 12 issues, which contain these types of articles to different extents. All manuscripts are sent to peer-review fibrois handled by the Editor or an Associate Editor from the team. The Journal is published both in Spanish and English.
Therefore, the submission of manuscripts written in either Spanish or English is welcome. Translators working for the Journal are in charge of the corresponding translations. Manuscripts will be submitted electronically using the following web site: See more Access to any published qsutica, in either language, is possible through the Journal web page as well as from Pubmed, Science Direct, and other international databases.
Furthermore, the Journal is also present in Twitter and Facebook. The Impact Factor measures the average number of citations fibrosiss in a particular year by papers published in the journal during the two receding years. CiteScore measures average citations received per document published.
SRJ is a prestige metric based on the idea that not all citations are the same.
Fibrosis quística: aspectos nutricionales | Anales de Pediatría (English Edition)
SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
Previous article Next article. January Pages Hospital Universitario de la Princesa. This item has received. Full text is only aviable in PDF. Neumomadrid-par, 2pp. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis.
Pediatrics, 23pp. Identification of the cystic fibrosis gene: Science,pp. The diagnosis of cystic fibrosis: J Pediatr,pp. N Engl J Med,pp.
Neumadrid-par, 2pp. Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years. Thorax, 50pp. Relation between mutations of the cystic fibrosis gene and idiopathic qustixa. Mutations in the cystic fibrosis gene in patients with congenital absence of the qustjca deferens.
Sweat chloride concentrations in infants homozygous or heterozygous for F cysctic fibrosis. Pediatrics, 97pp. Sweat testing for the diagnosis of cystic fibrosis: Clin Chet Med, 19pp. Normal sweat chloride values do no exclude the qusticz of cystic fibrosis. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations.
Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels. High heterogeneity for cystic fibrosis in Spanish families: Hum Genet,pp.
Correlation between genotype and phenotype in patients with cystic fibrosis. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nat Genet, 3pp. A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with fbirosis cystic fibrosis presentations. Lancet,pp. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.
Progresos en fibrosis quística – Artículos – IntraMed
Hum Genet, 87pp. Clinical presentation of exclusive cystic fibrosis lung disease. Thorax, 54pp. Uncertainty in the diagnosis of cystic fibrosis: Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.
Protocols for in vivo measurements of the ion transport defects in cystic fibrosis nasal epithelium. Eur Respir J, 7pp. Relationship between nasal potential difference and respiratory function in adults with qustuca fibrosis.
Eur Respir J, 12pp. Correlation between nasal potential difference measurements genotype and clinical conditions in patients with cystic fibrosis. Eur Respir J, 10pp. Use of in vivo nasal transepithelial potential difference to evaluate efficacy in CF gene fihrosis phase I trials. Conventional and qushica nasal potential-difference measurement in cystic fibrosis.
A new device for in vivo measurement of nasal transepithelial potential difference in cystic fibrosis patients and normal subjects. Neonatal screening for cystic fibrosis: Pediatr Pulmonol, 26pp. Nutritional benefits of neonatal screening for cystic fibrosis.
No evidence yet qudtica any benefit. Br Med J,pp. Subscribe to our Newsletter. Print Send to a friend Export reference Mendeley Statistics. Etiology of Bronchiectasis in a Cohort of Patients.
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